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Details

Stereochemistry EPIMERIC
Molecular Formula C34H62FN2O10PS
Molecular Weight 740.901
Optical Activity UNSPECIFIED
Defined Stereocenters 4 / 5
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of FOSFLURIDINE TIDOXIL

SMILES

CCCCCCCCCCCCSCC(COP(O)(=O)OC[C@H]1O[C@H]([C@H](O)[C@@H]1O)N2C=C(F)C(=O)NC2=O)OCCCCCCCCCC

InChI

InChIKey=LBBDGLOPGRGFDO-FKJRLRTPSA-N
InChI=1S/C34H62FN2O10PS/c1-3-5-7-9-11-13-14-16-18-20-22-49-26-27(44-21-19-17-15-12-10-8-6-4-2)24-45-48(42,43)46-25-29-30(38)31(39)33(47-29)37-23-28(35)32(40)36-34(37)41/h23,27,29-31,33,38-39H,3-22,24-26H2,1-2H3,(H,42,43)(H,36,40,41)/t27?,29-,30-,31-,33-/m1/s1

HIDE SMILES / InChI

Molecular Formula C34H62FN2O10PS
Molecular Weight 740.901
Charge 0
Count
Stereochemistry EPIMERIC
Additional Stereochemistry No
Defined Stereocenters 4 / 5
E/Z Centers 0
Optical Activity UNSPECIFIED

Flosfluridine tidoxil, a thymidylate synthase inhibitor that was developed for the treatment of actinic keratosis and solid tumors, e.g. breast and colorectal cancers. These studies were suspended and information about the further development of this drug is not available.

Approval Year

Substance Class Chemical
Created
by admin
on Mon Mar 31 18:42:39 GMT 2025
Edited
by admin
on Mon Mar 31 18:42:39 GMT 2025
Record UNII
VY3U311S3Q
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
5'-URIDYLIC ACID, 5-FLUORO-, MONO(2-(DECYLOXY)-3-(DODECYLTHIO)PROPYL) ESTER
Preferred Name English
FOSFLURIDINE TIDOXIL
INN  
INN  
Official Name English
5-FLUOROURIDINE 5'-((2RS)-2-(DECYLOXY)-3-(DODECYLSULFANYL)PROPYL HYDROGEN PHOSPHATE)
Systematic Name English
fosfluridine tidoxil [INN]
Common Name English
Code System Code Type Description
CAS
174638-15-4
Created by admin on Mon Mar 31 18:42:39 GMT 2025 , Edited by admin on Mon Mar 31 18:42:39 GMT 2025
PRIMARY
PUBCHEM
9875280
Created by admin on Mon Mar 31 18:42:39 GMT 2025 , Edited by admin on Mon Mar 31 18:42:39 GMT 2025
PRIMARY
SMS_ID
300000036930
Created by admin on Mon Mar 31 18:42:39 GMT 2025 , Edited by admin on Mon Mar 31 18:42:39 GMT 2025
PRIMARY
FDA UNII
VY3U311S3Q
Created by admin on Mon Mar 31 18:42:39 GMT 2025 , Edited by admin on Mon Mar 31 18:42:39 GMT 2025
PRIMARY
ChEMBL
CHEMBL2107800
Created by admin on Mon Mar 31 18:42:39 GMT 2025 , Edited by admin on Mon Mar 31 18:42:39 GMT 2025
PRIMARY
EPA CompTox
DTXSID50938541
Created by admin on Mon Mar 31 18:42:39 GMT 2025 , Edited by admin on Mon Mar 31 18:42:39 GMT 2025
PRIMARY
INN
8613
Created by admin on Mon Mar 31 18:42:39 GMT 2025 , Edited by admin on Mon Mar 31 18:42:39 GMT 2025
PRIMARY
NCI_THESAURUS
C170009
Created by admin on Mon Mar 31 18:42:39 GMT 2025 , Edited by admin on Mon Mar 31 18:42:39 GMT 2025
PRIMARY
Related Record Type Details
ACTIVE MOIETY